Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750042
rs63750042
0.710 GeneticVariation BEFREE Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing. 19669601

2009

dbSNP: rs63750042
rs63750042
T 0.710 CausalMutation CLINVAR